Clinical questions - Gastroenterology Flashcards

(33 cards)

1
Q

Distinguishing between upper and lower GI bleeds

A

UGI is typically melenic stools
LGI is typically red blood or hematochezia

Ligament of Treitz is the landmark dividing upper and lower

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2
Q

Most important aspect of managing an acute, large volume GI bleed

A

IVF resuscitation

Hypotension surpasses all other findings - you have to perfuse the body

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3
Q

HBsAg -
HBsAb -
HBcAB +
HBeAg -

A

Window period

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4
Q

HBsAg +
HBsAb -
HBcAB +
HBeAg +

A

Acute disease

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5
Q

HBsAg -
HBsAb +
HBcAB +
HBeAg -

A

Recovered

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6
Q

HBsAg -
HBsAb +
HBcAB -
HBeAg -

A

Vaccinated

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7
Q

Ulcerative colitis (presentation, lab markers, endoscopy findings, treatment)

A

Presentation: intermittently bloody diarrhea with colicky abdominal pain and fatigue

Labs: pANCA positive

Scope: continuous circumferential inflammation of the rectum that may include more proximal colon

Treatment:
Mild/all patients: 5-ASA (mesalamine) can be given orally or suppositories or enemas

More severe disease:

  • Steroids
  • Immunosuppressants: cyclosporine, azathioprine, 6-mercaptopurine
  • Anti-TNFalpha durgs: infliximab

Colectomy is curative

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8
Q

Cause of diarrhea in a patient with HIV and CD4 less than 100

A

Cryptosporidium

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9
Q

Cause of diarrhea in a patient with vomiting and diarrhea after eating reheated Chinese fried rice

A

Bacillus cereus

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10
Q

Cause of diarrhea in a patient with vomiting and diarrhea after eating raw oysters

A

Vibrio parahaemolyticus

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11
Q

Cause of diarrhea in a patient with diarrhea beginning after backpacking in the mounts

A

Giardia lamblia

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12
Q

Cause of diarrhea in a patient with recent treatment for UTI

A

C. diff

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13
Q

Type of hepatitis with AST 2 times as high as ALT

A

Alcohol hepatitis

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14
Q

In general, causes of direct vs indirect hyperbilirubinemia

A

Direct (conjugated) bilirubin is elevated in hepatobiliary disease

Indirect (unconjugated) bilirubin is elevated in hemolysis

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15
Q

Crohn disease (presentation, lab markers, endoscopy, treatment)

A

Colicky abdominal pain, occasional low grade fevers

Lab: ASCA (Anti-Saccharomyces cerevisiae antibodies) positive (ANCAs negative)

Scope: cobblestoning and skip lesions
Path: transmural inflammation, non-caseating granulomas

Treatment:
5-ASA
Steroids
Immunosuppressants
Anti-TNF alpha drugs

Colectomy no curative in Crohn dz

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16
Q

Irritable bowel syndrome

A

Intermittent abdominal bloating and crampy lower abdominal pain without nausea or vomiting; alternating between diarrhea and constipation with defecation often relieving the abdominal pain. No blood or mucus in stools

Tx:
Avoid gas producing foods
Diet low in fermentable short chain saccharides (lactose, fructose)
GF diet
High fiber diet
Exercise
17
Q

Celiac disease

A

Chronic diarrhea - steatorrhea
Occasional nausea/vomiting and abdominal pain

Lab markers: anti-endomysial Ab and anti-tissue transglutaminase Ab positive

GF diet: “BROW” - barley, rye, oats (often contaminated), wheat

18
Q

Hereditary Hemochromatosis

A

AR - increased Fe absorption

Presentation: pruritis, jaundice, fatigue, infertility, joint pain, fat malabsorption

Advanced disease: skin hyperpigmentation, DM, cirrhosis
-“Bronze diabetes”

Labs: elevated Fe, ferritin, transferrin, %sat; decreased TIBC

Dx: Liver biopsy
Most common - HFE gene mutation

Tx: phlebotomy

19
Q

Criteria to use ppx against stress ulcers in the ICU

A
Coagulopathy
intubation/ventillation > 48 hrs
GI ulceration/bleeding within 1 yr
Head trauma
Spinal cord trauma
burn injury
2 or more of the following:
Sepsis
ICU > 1 week
Occult GI bleed 6 or more days
Glucocorticoid tx
20
Q

What infectious risk is associated with PPIs and H2 blockers

A

C diff risk increased

21
Q

Acute pancreatitis: presentation, an Initial lab testing, an Initial lab testing, management

A

Presentation: epigastric pain, nausea, vomiting, anorexia
Exam: epigastric tenderness without guarding, may have ecchymosis at bilateral flanks (Grey-turner sign) or at umbilicus ( Cullen sign)

Lab: elevated serum lipase

Management:
Admit +/- ICU
Monitor for hemodynamic instability and organ failure
Aggressive hydration
NPO
Pain control (morphine)
Established underlying cause

If worsening, CT A/P to r/o pseudocyst

22
Q

Common causes of pancreatitis

A

Most common - gallstone
Alcohol abuse
Medications
Elevated triglycerides

23
Q

Causes of cirrhosis and portal vein hypertension

A
Alcohol abuse
Chronic hepatitis B or C
Fatty liver disease
Hemachromatosis
Chronic biliary obstruction
Chronic cholestasis
24
Q

Exam findings consistent with cirrhosis

A

Jaundice, spider angiomata, gynecomastia, abdominal distention with shifting dullness and a fluid wave

25
Lab testing to determine cause of ascitic fluid
Serum albumin compared with ascitic fluid albumin Calculate SAAG > or = 1.1 - cirrhosis, CHF, budd chiari (portal vein thrombosis) less than 1.1 - pancreatitis, chronic nephrotic syndrome (losing protein)
26
Achalasia - presentation, diagnosis and management
Presentation: Progressive difficulty swallowing to both liquids and solids, with a sensation of sticking in chest Barium esophageal shows narrowing of the esophagogastric junction - "bird's beak" appearance, with a dilation of the proximal esophagus Confirm diagnosis with esophageal manometry - high LES pressure, lack peristaltic distally Tx: Esophageal dilation Surgical myotomy Botox to LES Medical tx: nifedipine, nitrates
27
Primary sclerosing cholangitis - cause, presentation, diagnosis, tx, risk
Inflammation and stricturing of the biliary tree, leading to cholestasis, jaundice, and pruritic - Common in young men, hx of IBD esp. UC Lab: elevated direct bill and ALP pANCA strongly positive (30-80:1) ERCP with beads on a string Tx: No proven medical treatment ERCP for a dominant stricture - dilate Liver transplant for advanced liver disease and cirrhosis Risk: cholangiocarcinoma, gallbladder cancer, hepatocellular carcinoma (2/2 cirrhosis)
28
gastritis management
Get EGD to r/o gastric CA with bx Tx: PPI triple antibiotic tx if H. pylori cause Limit use of NSAIDs, tobacco, etoh
29
alpha 1 antitrypsin deficiency
Increased elastase activity leads to lung disease - panacinar emphysema - obstructive pattern on PFTs Mutated protein accumulates in the liver which is toxic to the cells -> liver disease - early onset cirrhosis Tx: - infusion of alpha 1 antitrypisn (A1AT) - Lung transplant - liver transplant is curative as it makes normal alpha1 antitrypsin
30
Treatment for c. diff
Most common initial therapy is metronidazole If initial therapy fails or recurrent diarrhea or more severe: - PO Vanc - Fidoxamicin - rifaximin - fecal bacteriotherapy - enema
31
Primary biliary cirrhosis - presentation, exam findings, diagnosis, management
Presents with generalized pruritic, fatigue, RUQ pain Associated with other autoimmune disorders, middle aged females - 90% Exam: mild hyperpigmentation of skin without jaundice or scleral icterus (unless advanced then + jaundice) Liver moderately enlarged - contender ``` Labs: Mild elevated AST, ALT markedly elevated ALP normal t bili ANA (antinuclear) and AMA (antimitochondrial) Ab positive ``` Confirm dx: liver bx Tx: - Ursodeoxycholic acid - cholestyramine for pruritis - ultimately transplant
32
Treatment of GERD
mild - lifestyle modifications: Weight loss, elevate head of bed, stop smoking, limit alcohol, caffeine, chocolate, avoid eating 3 to 4 hours before bed next option: H2 blocker or PPI
33
Wilson's disease
Effects liver, brain, eyes Exam: Kayser Fleischer rings on slip lamp exam Labs: - slightly elevated AST, ALT - normal t bili, ALP - ferritin normal - Serum ceruloplasmin low or normal -> low serum copper - high 24 hr urine copper Dx: liver bx genetic testing - multiple mutations Tx: Chelation - penicillamine or trientine